FDA.reportPublic FDA data

ZIMS MAX FREEZE

Manufacturer
NATURAL ESSENTIALS, INC.
Effective date
2018-01-01
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-01 22:23:40

Label at a glance#

ProductZIMS MAX FREEZE
Active ingredientMENTHOL, UNSPECIFIED FORM
Label structure11 sections

Dosage and administration

Adults and children 12 years and older Apply and gently massage painful joint and/or muscles. Repeat as needed no more than 4 times a day. Wash hands after each use with cold water.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Natural Menthol USP 3.7%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Use

INDICATIONS & USAGE SECTION

  • For the temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthritis, strains, bruises and sprains.

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

  • if you are allergic to any ingredient in Zim's Max-Freeze
  • on open wounds, damaged or irritated skin
  • in large quantities, particularly on raw surfaces or blistered areas

Ask a doctor or pharmacist before use if you are

OTC - ASK DOCTOR/PHARMACIST SECTION

  • using blood thinning medications, steroids or non-steroidal anti-inflammatory drugs (NSAIDS)

When using this product

OTC - WHEN USING SECTION

  • do not use other topical products
  • do not use with heating devices
  • avoid contact with eyes or mucous membranes
  • do not bandage tightly
  • keep away from excessive heal

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition worsens or
  • symptoms persist for more than 7 days or dear up and occur again within a few days

PREGNANCY SECTION

If pregnant or breast feeding ask a physician before use

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If put in the mouth, got medical help or contact a poison control center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years and older

  • Apply and gently massage painful joint and/or muscles.
  • Repeat as needed no more than 4 times a day.
  • Wash hands after each use with cold water.

Other information

OTHER SAFETY INFORMATION

Store at room temperature - do not exceed 86° Fahrenheit, 30° Celsius.

Inactive ingredients

INACTIVE INGREDIENT SECTION

†Aloe Barbadensis Leaf Extract, Arnica Extract, Camphor, Carbomer, Ethylhexylglycerin, †Ilex Paraguarionsis Leaf Extract, Isopropyl Alcohol, Phenoxyethanol, Tea Tree Oil, Tocopheryl Acetate (Vitamin E Acetate), Triethanolamine, Water.

†Symbol before the ingredient indicates certified organic.

Principal Display Panel - 4 oz Tube Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ZIMS®

MAX FREEZE

MUSCLE & JOINT*

Greaseless, vanishing scent formula.
Organic ilex & aloe, arnica,
vitamin e and tea tree oil.
Paraben & sulfate free.

Nature Science

Net Wt 4 oz. (113.4g)

Principal Display Panel - 4 oz Tube Label
Principal Display Panel - 4 oz Tube Label

Principal Display Panel - 3 oz Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ZIMS®

MAX FREEZE

MUSCLE & JOINT*

Greaseless, vanishing scent
formula. Organic ilex & aloe,
arnica, vitamin e and tea tree oil.

Nature Science

89 mL (3 fl oz)

Principal Display Panel - 3 oz Bottle Label
Principal Display Panel - 3 oz Bottle Label

PRINCIPAL DISPLAY PANEL - 5 g SAMPLE Pouch Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ZIM'S®
MAX-
FREEZE

PAIN RELIEF

Greaseless, vanishing scent formula.
Organic ilex & aloe, arnica,
vitamin e and tea tree oil.
Paraben & sulfate free.

Nature Science

ZimsUSA.com
5g SAMPLE

PRINCIPAL DISPLAY PANEL - 5 g SAMPLE Pouch Label
PRINCIPAL DISPLAY PANEL - 5 g SAMPLE Pouch Label

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
66902-01466902-014-04, 66902-014-03
66902-40066902-400-05

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 24 matching rows.

Name, UNII, Kind table
NameUNIIKind
MENTHOL, UNSPECIFIED FORML7T10EIP3AACTIB
ALOE VERA LEAFZY81Z83H0XIACT
ARNICA MONTANA WHOLEO80TY208ZWIACT
CAMPHOR (SYNTHETIC)5TJD82A1ETIACT
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED)4Q93RCW27EIACT
ILEX PARAGUARIENSIS LEAF1Q953B4O4FIACT
ISOPROPYL ALCOHOLND2M416302IACT
PHENOXYETHANOLHIE492ZZ3TIACT
TEA TREE OILVIF565UC2GIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
TROLAMINE9O3K93S3TKIACT
WATER059QF0KO0RIACT
MENTHOL, UNSPECIFIED FORML7T10EIP3AACTIB
ALOE VERA LEAFZY81Z83H0XIACT
ARNICA MONTANA WHOLEO80TY208ZWIACT
CAMPHOR (SYNTHETIC)5TJD82A1ETIACT
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED)4Q93RCW27EIACT
ILEX PARAGUARIENSIS LEAF1Q953B4O4FIACT
ISOPROPYL ALCOHOLND2M416302IACT
PHENOXYETHANOLHIE492ZZ3TIACT
TEA TREE OILVIF565UC2GIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
TROLAMINE9O3K93S3TKIACT
WATER059QF0KO0RIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
1b28eb92-5661-4cdd-8e58-dffc8802b4bac85b499a-bb7a-4fc1-9401-4966d7e2a07e2018-01-01WarningsExact identifier
spl id: 1b28eb92-5661-4cdd-8e58-dffc8802b4ba
spl set id: c85b499a-bb7a-4fc1-9401-4966d7e2a07e

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.